TY - JOUR
T1 - Genomic insights into two colistin-resistant klebsiella pneumoniae strains isolated from the stool of preterm neonate during the first week of life
AU - Yap, Polly Soo Xi
AU - Ahmad Kamar, Azanna
AU - Chong, Chun Wie
AU - Ngoi, Soo Tein
AU - Teh, Cindy Shuan Ju
N1 - Funding Information:
This study was funded by University of Malaya Research Grant (UMRG: RG353-13HTM) and Postgraduate Research Funding (PPP: PG179-2015A).
Publisher Copyright:
© Copyright 2020, Mary Ann Liebert, Inc., publishers 2020.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/3
Y1 - 2020/3
N2 - Background: Klebsiella pneumoniae is a major opportunistic pathogen frequently associated with nosocomial infections, and often poses a major threat to immunocompromised patients. In our previous study, two K. pneumoniae (K36 and B13), which displayed resistance to almost all major antibiotics, including colistin, were isolated. Both isolates were not associated with infection and isolated from the stools of two preterm neonates admitted to the neonatal intensive care unit (NICU) during their first week of life. Materials and Methods: In this study, whole genome sequencing was performed on these two clinical multidrug resistant K. pneumoniae. We aimed to determine the genetic factors that underline the antibiotic-resistance phenotypes of these isolates. Results: The strains harbored blaSHV-27, blaSHV-71, and oqxAB genes conferring resistance to cephalosporins, carbapenems, and fluoroquinolones, respectively, but not harboring any known plasmid-borne colistin resistance determinants such as mcr-1. However, genome analysis discovered interruption of mgrB gene by insertion sequences gaining insight into the development of colistin resistance. Conclusion: The observed finding that points to a scenario of potential gut-associated resistance genes to Gram negative (K. pneumoniae) host in the NICU environment warrants attention and further investigation.
AB - Background: Klebsiella pneumoniae is a major opportunistic pathogen frequently associated with nosocomial infections, and often poses a major threat to immunocompromised patients. In our previous study, two K. pneumoniae (K36 and B13), which displayed resistance to almost all major antibiotics, including colistin, were isolated. Both isolates were not associated with infection and isolated from the stools of two preterm neonates admitted to the neonatal intensive care unit (NICU) during their first week of life. Materials and Methods: In this study, whole genome sequencing was performed on these two clinical multidrug resistant K. pneumoniae. We aimed to determine the genetic factors that underline the antibiotic-resistance phenotypes of these isolates. Results: The strains harbored blaSHV-27, blaSHV-71, and oqxAB genes conferring resistance to cephalosporins, carbapenems, and fluoroquinolones, respectively, but not harboring any known plasmid-borne colistin resistance determinants such as mcr-1. However, genome analysis discovered interruption of mgrB gene by insertion sequences gaining insight into the development of colistin resistance. Conclusion: The observed finding that points to a scenario of potential gut-associated resistance genes to Gram negative (K. pneumoniae) host in the NICU environment warrants attention and further investigation.
KW - colistin resistance
KW - Klebsiella pneumoniae
KW - multidrug resistant bacteria
KW - polymyxin
KW - preterm infants
KW - virulence
KW - whole-genome sequencing
UR - http://www.scopus.com/inward/record.url?scp=85081685025&partnerID=8YFLogxK
U2 - 10.1089/mdr.2019.0199
DO - 10.1089/mdr.2019.0199
M3 - Article
C2 - 31545116
AN - SCOPUS:85081685025
SN - 1076-6294
VL - 26
SP - 190
EP - 203
JO - Microbial Drug Resistance
JF - Microbial Drug Resistance
IS - 3
ER -